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Quality Engineer - County Sligo.Key Responsibilities:• Provide technical quality support to Project Manager, Design Engineers, Production Manager and clients.• Work closely with Engineering team and the client to establish and maintain compliant product specifications.• Quality review of process val...

Quality Engineer - County Sligo.Key Responsibilities:• Provide technical quality support to Project Manager, Design Engineers, Production Manager and clients. • Work closely with Engineering team and the client to establish and maintain compliant product specifications. • Quality review of process v...

Quality Specialist - Dublin 12/hybridRole Overview:As a Quality Assurance Specialist, your primary duties will revolve around maintaining and enhancing the quality systems to ensure compliance with industry standards, regulatory requirements, and internal procedures. You will work closely with the Q...

A Principal Scientist – QC Compliance is required on a PERMANENT basis by CareerWise Recruitment for our Limerick based start-up Biopharmaceutical Client.The Senior Scientist Compliance role in Quality Control provides technical support for the compliance systems within the quality control laborator...

A Process Engineer P2 is required on an initial 11-Month contract basis by CareerWise Recruitment for our Carlow-based multinational bio-pharmaceutical client.Hybrid – Day role with expectation to support shift intermittently when Floor activities/studies are ongoing.The successful candidate will se...

Principal Scientist - Quality Control ComplianceLocation: Limerick, IrelandCompany: Leading Biopharma CompanyAbout Us:Join a pioneering biopharma company at the forefront of healthcare innovation in Limerick, Ireland. Our state-of-the-art facility, currently under construction, will be one of the mo...

Principal/Senior Principal Downstream Bioprocess Scientist - Technical Services/Manufacturing SciencesRole Overview:The Principal/Senior Principal Downstream Bioprocess Scientist - TS/MS will play a pivotal role in introducing and supporting manufacturing processes within the downstream operations e...

A Technical Writer is required by CareerWise Recruitment to work with a Cork based multinational on a minimum 6 month contract position. Attractive hourly rate on offer.THE ROLE:*Perform technical writing activities and assist the project engineers in the generation of validation documentations.* Up...

Quality Assurance (QA) Associate – Training and Qualification required for pharma client based in Limerick.Responsibilities: Training Program Development: Design, develop, and update training materials, curricula, and assessments, with an emphasis on creating engaging video content and interactive...

Manufacturing EngineerLocation: Clonmel, IrelandOverview:Are you passionate about engineering and eager to contribute to groundbreaking healthcare solutions? I am currently recruiting for an exciting opportunity with a leading healthcare company, where you’ll join their esteemed Vascular Division in...

Senior Product Design EngineerLocation: Clonmel, Ireland (Hybrid Work Position)Division: VascularCompany Overview: We are a leading healthcare company with almost 3,000 employees across 10 sites in Ireland. Our diverse product range includes diagnostics, medical devices, nutritionals, and branded ge...

Product Quality Professional - North Dublin.Core tasks and responsibilities:• Contributing and leading in a broad range of activities including process change, risk assessment, CAPA, non-conforming material, complaint handling, manufacturing process deviations, non-conformance handling and validatio...

A Technical Transfer Engineer  is required by CareerWise Recruitment for a Biotechnology client. This is a 12-month contract. Must Have Drug Substance Biologics Monoclonal Antibodies  Technical Transfer Experience .This is a remote based position with 10% travel to Germany (you would  have to be liv...

A Quality Specialist is required by CareerWise Recruitment for our Dublin 12 based client. Reporting to the Quality Manager, the ideal candidate will have 3 - 5 years’ experience in a Pharmaceutical/ Regulated background with strong working knowledge of GMP, regulatory expectations, and familiarity...